BEUDAMED
    FDA Adverse Event Death Summary report: N

    RIS

    MDR report key: 448832 · Received March 18, 2003

    Report

    Report Number
    1219343-2003-00002
    Event Type
    Death
    Date Received
    March 18, 2003
    Date of Event
    February 22, 2002
    Report Date
    March 18, 2003
    Manufacturer
    HAEMONETICS CORP.
    Product Code
    CAC
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT DEATH. NO SPECIFIC INFORMATION WHETHER DEVICE WAS INVOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RIS AUTOTRANSFUSION SYSTEM CAC HAEMONETICS CORP. RIS NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death